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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Sonrisas canónicas | C1CCN(CC1)C(=O)N2CCN(CC2)CC(=O)NC3=C(C=CC(=C3)Cl)Cl |
|---|---|
| IUPAC Name | N-(2,5-dichlorophenyl)-2-[4-(piperidine-1-carbonyl)piperazin-1-yl]acetamide |
| InChIKey | CXAWUJLFURNRTD-UHFFFAOYSA-N |
| INCHI | 1S/C18H24Cl2N4O2/c19-14-4-5-15(20)16(12-14)21-17(25)13-22-8-10-24(11-9-22)18(26)23-6-2-1-3-7-23/h4-5,12H,1-3,6-11,13H2,(H,21,25) |
| Peso molecular | 399.300 |
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Clase | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives |
| Direct Parent | Alpha amino acid amides |
| Alternative Parents | N-piperazineacetamides Anilides Piperazine carboxamides Piperidinecarboxamides N-arylamides Dichlorobenzenes N-alkylpiperazines Aryl chlorides Ureas Secondary carboxylic acid amides Trialkylamines Azacyclic compounds Organopnictogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Alpha-amino acid amide - N-piperazineacetamide - Piperazine-1-carboxamide - Anilide - 1-piperidinecarboxamide - Piperidinecarboxamide - 1,4-dichlorobenzene - N-arylamide - Chlorobenzene - Halobenzene - N-alkylpiperazine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - 1,4-diazinane - Piperazine - Benzenoid - Piperidine - Urea - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Carbonic acid derivative - Carboxamide group - Azacycle - Organoheterocyclic compound - Amine - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organohalogen compound - Carbonyl group - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as alpha amino acid amides. These are amide derivatives of alpha amino acids. |
| External Descriptors | Not available |
| Peso molecular | 399.300 g/mol |
|---|---|
| XLogP3 | 2.600 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 3 |
| Exact Mass | 398.128 Da |
| Monoisotopic Mass | 398.128 Da |
| Topological Polar Surface Area | 55.900 Ų |
| Heavy Atom Count | 26 |
| Formal Charge | 0 |
| Complexity | 494.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |